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"Mutation, hereditary"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´(Áõ)
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ, À¯Àü´Ù¹ß¿Ü°ñÁõ
  • hereditary mutilating keratoma
    À¯ÀüÀý´Ü°¢È­Á¾
  • hereditary nonpolyposis colorectal cancer
    1. À¯Àü¼ººñÆú¸³À߷ϰðâÀÚ¾Ï 2. À¯Àü¼ººñÆú¸³´ëÀå¾Ï
  • hereditary opalescent dentine
    À¯ÀüÁ¥ºû»ó¾ÆÁú
  • hereditary palmoplantar keratoderma
    À¯Àü¼Õ¹ß¹Ù´Ú°¢ÁúÇǺÎÁõ
  • hereditary spastic paraplegia
    À¯Àü°­Á÷ÇϹݽŸ¶ºñ
  • hereditary spherocytosis
    À¯Àü°ø¸ð¾çÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
  • hereditary tremor
    À¯Àü¶³¸²
  • hereditary tubulointerstitial nephritis
    À¯Àü¿ä¼¼°ü»çÀÌÁúÄáÆÏ¿°, À¯Àü¿ä¼¼°ü°£Áú½ÅÀå¿°
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • allelic mutation
    ¸Â¼¶µ¹¿¬º¯ÀÌ, ´ë¸³µ¹¿¬º¯ÀÌ
  • back mutation
    ¿ªµ¹¿¬º¯ÀÌ, º¹±Íµ¹¿¬º¯ÀÌ
  • cold-sensitive mutation
    Àú¿Â¹Î°¨µ¹¿¬º¯ÀÌ, Àú¿Â°¨¼ö¼ºµ¹¿¬º¯ÀÌ
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  • ¿µ¹®
    ÇѱÛ
  • hereditary leptocytosis
    À¯ÀüÇ¥ÀûÀûÇ÷±¸Áõ
  • hereditary lymphedema
    À¯Àü¸²ÇÁºÎÁ¾
  • hereditary spherocytosis
    À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
  • hereditary stigma
    À¯Àü¡ǥ
  • hereditary syphilis
    (¢¡congenital syphilis) ¼±Ãµ¸Åµ¶
  • hereditary trait
    À¯Àü¼ÒÁú
  • hereditary tremor
    (¢¡essential tremor) º»Å¶³¸², À¯Àü¶³¸², ¿øÀθ𸦶³¸²
  • hereditary adrenogenital syndrome
    À¯ÀüºÎ½Å¼º±âÁõÈıº
  • hereditary hemorrhagic telangiectasia
    À¯ÀüÃâÇ÷¸ð¼¼Ç÷°üÈ®ÀåÁõ, À¯ÀüÃâÇ÷½ÇÇÍÁÙÈ®ÀåÁõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • hereditary mutilating keratoma
    À¯ÀüÀý´Ü°¢È­Á¾
  • hereditary palmoplantar keratoderma
    À¯Àü¼Õ¹ß¹Ù´Ú°¢ÁúÇǺÎÁõ
  • hereditary pyloric stenosis
    À¯Àü³¯¹®ÇùÂø
  • hereditary spastic paraplegia
    À¯Àü°æÁ÷ÇϹݽŸ¶ºñ
  • hereditary tubulointerstitial nephritis
    À¯Àü´¢¼¼°ü»çÀÌÁúÄáÆÏ¿°
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • hereditary adrenogenital syndrome
    À¯Àü¼º ºÎ½Å¼º±â¼º ÁõÈıº.
  • hereditary angioedema
    À¯Àü¼º ¸Æ°üºÎÁ¾
  • hereditary angioedema
    À¯Àü¼ºÇ÷°üºÎÁ¾
  • hereditary aphasia
    À¯Àü(¼º) ½Ç¾î(Áõ).
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¼º ¾ç¼º »óÇdz» ÀÌ»ó°¢È­Áõ
  • hereditary brown enamel
    À¯Àü¼º °¥»ö ¹ý³¶Áú.
  • hereditary brown tooth
    À¯Àü¼º °¥»öÄ¡¾Æ.
  • hereditary bullous epidermolysis ³ª e.bullosa hereditaria
    À¯Àü¼º Ç¥ÇǼöÆ÷Áõ.
  • hereditary cerebellar ataxia
    À¯Àü¼º ¼Ò³ú¼º ¿îµ¿½ÇÁ¶.
  • hereditary cerebellar sclerosis
    À¯Àü¼º ¼Ò³ú°æÈ­Áõ.
  • hereditary cerebral hemorrhages with amyloidosis(hchwa)
    À¯Àü¼º ³úÃâÇ÷, ¾Æ¹Ð·ÎÀ̵åÁõ¼º
  • hereditary chorea
    À¯Àü(¼º) ¹«µµº´.
  • hereditary coagulation disorder
    À¯Àü¼º ÀÀ °íÀå¾Ö.
  • hereditary coproporphyria
    À¯Àü¼º ÄÚÇÁ·ÎÆ÷ ¸£ÇǸ®¾Æ.
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  • ¿µ¹®
    ÇѱÛ
  • gene mutation
    À¯ÀüÀÚ(µ¹¿¬)º¯ÀÌ
  • genetic mutation
    À¯ÀüÀû µ¹¿¬º¯ÀÌ
  • genomic mutation
    À¯ÀüÀÚµ¹¿¬º¯ÀÌ
  • host range mutation
    ¼÷ÁÖ¿ªº¯ÀÌ
  • induced mutation
    À¯¹ß¼º µ¹¿¬º¯ÀÌ.
  • induced mutation
    À¯¹ßµ¹¿¬º¯ÀÌ
  • lethal mutation
    Ä¡»çµ¹¿¬º¯ÀÌ(¡­ÔÍæ×ܨì¶).
  • lethal mutation
    Ä¡»ç µ¹¿¬º¯ÀÌ
  • loss mutation
    »ó½Çµ¹¿¬º¯ÀÌ(ßÃã÷ÔÍæÔܨì¶).
  • missense mutation
    °ú¿Àµ¹¿¬º¯ÀÌ(Φè¦ÔÍæÔܨì¶).
  • multiple allelic mutation
    º¹´ë¸³ÇüÁúº¯ÀÌ(ÜÜÓßí¡û¡òõܨì¶).
  • mutation
    (µ¹¿¬)º¯ÀÌ(ÔÍæÔܨì¶)
  • mutation detection
    (µ¹¿¬)º¯À̰ËÃâ
  • mutation disturbance
    º¯¼ºÀå¾Ö(ܨàõî¡äô).
  • mutation genetics
    º¯ÀÌÀ¯ÀüÇÐ(ܨì¶ë¶îîùÊ).
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  • isocoding mutation
    ¾ÆÀ̼ÒÄÚµå º¯ÀÌ(ܨì¶)
  • Jimpy mutation
    ÁüÇÇ º¯ÀÌ(ܨì¶)
  • lethal mutation
    Ä¡»çº¯ÀÌ(öÈÞÝܨì¶)
  • lethal mutation model
    Ä¡»çº¯ÀÌ(öÈÞÝܨì¶)¸ðµ¨
  • missense mutation
    ¿ÀÀκ¯ÀÌ(è¦ìãܨì¶)
  • mutation
    º¯ÀÌ(ܨì¶)
  • mutation distance
    º¯ÀÌ(ܨì¶)°Å¸®
  • mutation frequency
    º¯À̺óµµ(ܨì¶ÞºÓø)
  • mutation index
    º¯ÀÌÁö¼ö(ܨì¶ò¦â¦)
  • mutation rate
    º¯ÀÌÀ²(ܨì¶ëÒ)
  • mutation stabilization
    º¯À̾ÈÁ¤È­(ܨì¶äÌïÒûù)
  • mutation theory
    º¯ÀÌ·Ð(ܨì¶Öå)
  • neutral mutation
    Á߸³º¯ÀÌ(ñ騡܍ì¶)
  • nonsense mutation
    ³Í¼¾½º º¯ÀÌ(ܨì¶)
  • ochre mutation
    ¿À¿ìÄ¿º¯ÀÌ(ܨì¶)
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HCP Hereditary Copro-Porphyria; À¯Àü¼º CoproPorphyria
HEMPAS Test Hereditary Erythrocytic Multinuclearity with Positive Acidified Serum Test
HMSN Hereditary Motor-Sensory Neuropathy
HPP Hereditary Pyro-Poikilocytosis
HS Hereditary Spherocytosis
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
MCR mutation cluster region
M(f) mutation frequency
Tfm testicular feminization mutation
AHO Albright hereditary osteodystrophy
CHED Congenital Hereditary Endothelial Dystrophy
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    ÇѱÛ
    ¼³¸í
  • hereditary opalescent dentin
    À¯Àü¼º À¯¹é»ö »ó¾ÆÁú
    »ó¾ÆÁú Çü¼º ºÎÀüÁõ¿¡ ³ªÅ¸³ª´Â À¯¹é±¤À» ¹ß»êÇÏ´Â °Í °°ÀÌ º¸ÀÌ´Â °¥»öÀÇ »ó¾ÆÁú.
  • hereditary porphyria cutanea tarda
    À¯Àü¼º ¸¸¹ß¼º ÇǺΠÆ÷¸£ÇǸ°Áõ
  • hereditary syphilis
    ¼±Ãµ ¸Åµ¶
    µ¿ÀǾî=congenital sy
  • hereditary telangiectasia
    À¯Àü¼º ¸ð¼¼Ç÷°ü È®ÀåÁõ
    ¼±ÃµÀûÀ¸·Î ¸ð¼¼Ç÷°üÀÌ È®ÀåµÇ´Â ÁúȯÀ¸·Î °üÂû ½Ã ¹ÝÁ¡»ó È«¹ÝÀ¸·Î ³ªÅ¸³ª°í °³º°ÀûÀ¸·Î È®ÀåµÈ Ç÷°ü ¾ç»óÀ» °üÂûÇÒ ¼ö ÀÖ´Ù.
  • lebers hereditary optic neuropathy
    ·¹¹ö¾¾ ¼±Ãµ¼º ½Ã½Å°æº´Áõ
  • amber mutation
    ¾Ïº£¸£ µ¹¿¬º¯ÀÌ
  • auxotrophic mutation
    ¿µ¾ç ¿ä±¸ µ¹¿¬º¯ÀÌ
  • biochemical mutation
    »ýÈ­ÇÐÀû µ¹¿¬º¯ÀÌ
  • clear plaque mutation
    Åõ¸í ÇöóÅ© µ¹¿¬º¯ÀÌ
  • cold-sensitive mutation
    ÇÑ·© ¹Î°¨¼º µ¹¿¬º¯ÀÌ
  • conditional mutation
    Á¶°ÇºÎ µ¹¿¬º¯ÀÌ
  • constitutive mutation
    ±¸¼ºÀû µ¹¿¬º¯ÀÌ
  • frameshift mutation
    °ñ°Ý ±¸Á¶ À̵¿ µ¹¿¬º¯ÀÌ
  • homoetic mutation
    È£¸Þ¿À½Ã½º µ¹¿¬º¯ÀÌ
  • missense mutation
    ¹Ì½º¼¾½º µ¹¿¬º¯ÀÌ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
mutation 1. A change in form, quality or some other characteristic.
2. <genetics> A permanent transmissible change in the genetic material, usually in a single gene. Also, an individual exhibiting such a change. Also called (in classical genetics) a sport.
Origin: L. Mutatio from mutare = to change
(18 Nov 1997)
mutation rate The frequency with which a particular mutation appears in a population or the frequency with which any mutation appears in the whole genome of a population. Normally the context makes the precise use clear.
See: fluctuation analysis.
(18 Nov 1997)
private mutation A rare mutation found usually only in a single family or a small population. It is like a privately printed book.
(12 Dec 1998)
homeotic mutation <embryology, genetics> A mutation that causes an organism to develop a homologous body part or structure in place of the part or structure that should normally be there (for example, developing a hand in place of a foot).
(09 Oct 1997)
silent mutation Mutations that have no effect on phenotype because they do not affect the activity of the product of the gene, usually because of codon ambiguity.
(18 Nov 1997)
site specific mutation An alteration of the structure of a gene at a specific sequence, usually referring to experimentally produced changes in gene sequence.
(05 Mar 2000)
somatic mutation Mutation that occurs in the somatic tissues of an organism and that will not, therefore, be heritable, since it is not present in the germ line. Some neoplasia is due to somatic mutation, a more conspicuous example is the reversion of some branches of variegated shrubs to the wild type (completely green) phenotype. Somatic mutation is probably also important in generating diversity in V gene regions of immunoglobulins.
(18 Nov 1997)
somatic mutation theory of cancer That cancer is caused by a mutation or mutations in the body cells (as opposed to germ cells), especially nonlethal mutations associated with increased proliferation of the mutant cells.
(05 Mar 2000)
spontaneous mutation A mutation which occurs by itself without first being affected by a mutagen, for example during the process of DNA replication. Spontaneous mutations arise at a remarkably constant rate. The rate that spontaneous mutations arise has been used as an evolutionary clock to estimate how closely related two (or more) separate species are to each other.
(09 Oct 1997)
natural mutation A mutation which occurs by itself without first being affected by a mutagen, for example during the process of DNA replication. Spontaneous mutations arise at a remarkably constant rate. The rate that spontaneous mutations arise has been used as an evolutionary clock to estimate how closely related two (or more) separate species are to each other.
(09 Oct 1997)
neutral mutation A mutation that has no selective advantage or disadvantage. Considerable controversy surrounds the question of whether such mutations can exist.
(18 Nov 1997)
new mutation Redundant term for a heritable trait present in the offspring but in neither parent, i.e., not a pre-existing mutant form inherited.
(05 Mar 2000)
substitution mutation A mutation caused by a nucleotide base being replaced by a different one.
(09 Oct 1997)
nonsense mutation <molecular biology> A mutation that causes a polypeptide chain to be ended prematurely.
(13 Nov 1997)
null mutation Change in a gene that leads to nothing, for example to no enzyme or to a nonfunctioning enzyme.
(12 Dec 1998)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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